Search citation statements
Paper Sections
Citation Types
Year Published
Publication Types
Relationship
Authors
Journals
Background and AimsKlebsiella pneumoniae (K. pneumoniae), included in the World Health Organization's list of critical priority pathogens, is considered a serious threat to public health. The present study aims to investigate the prevalence of virulence‐associated and aminoglycoside resistance genes in clinical isolates of K. pneumoniae.MethodsThis cross‐sectional study was carried out on 88 clinical isolates of K. pneumoniae collected from patients at Zabol hospital, Iran. Isolates were identified using conventional microbiology tests and polymerase chain reaction (PCR). Antibiotic susceptibility patterns were ascertained by the disc diffusion method. The prevalence of virulence‐associated genes (K1, K2, K5, iucA, and peg‐344) and aminoglycoside resistance (AME) genes (aac (2′)‐Ia, aac (3)‐IIa, aac (3)‐Ib, aac (6′)‐1b, ant (2″)‐Ia, and aph (3″)‐Ib) was investigated by PCR.ResultsThe isolates were mostly resistant to kanamycin (73.8%) and streptomycin (69.3%). The most predominant virulence gene was iucA, observed in 89.8% of isolates, followed by peg‐344 55.7% and K5 14.8%. The most prevalent resistance gene was aph (3″)‐Ib, which was detected in 35.2% of isolates, followed by ant (2″)‐Ia 22.7% and aac (3)‐Ib 17%. In addition, sixteen different patterns of AME genes were observed.ConclusionMost investigated isolates of K. pneumoniae were positive for different virulence‐associated and AME genes and therefore can play a significant role in life‐threatening infections. Meanwhile, resistance rates to aminoglycoside antibiotics were high and it was primarily due to the presence of AME genes such as aph (3″)‐Ib, ant (2″)‐Ia, and aac (3)‐Ib.
Background and AimsKlebsiella pneumoniae (K. pneumoniae), included in the World Health Organization's list of critical priority pathogens, is considered a serious threat to public health. The present study aims to investigate the prevalence of virulence‐associated and aminoglycoside resistance genes in clinical isolates of K. pneumoniae.MethodsThis cross‐sectional study was carried out on 88 clinical isolates of K. pneumoniae collected from patients at Zabol hospital, Iran. Isolates were identified using conventional microbiology tests and polymerase chain reaction (PCR). Antibiotic susceptibility patterns were ascertained by the disc diffusion method. The prevalence of virulence‐associated genes (K1, K2, K5, iucA, and peg‐344) and aminoglycoside resistance (AME) genes (aac (2′)‐Ia, aac (3)‐IIa, aac (3)‐Ib, aac (6′)‐1b, ant (2″)‐Ia, and aph (3″)‐Ib) was investigated by PCR.ResultsThe isolates were mostly resistant to kanamycin (73.8%) and streptomycin (69.3%). The most predominant virulence gene was iucA, observed in 89.8% of isolates, followed by peg‐344 55.7% and K5 14.8%. The most prevalent resistance gene was aph (3″)‐Ib, which was detected in 35.2% of isolates, followed by ant (2″)‐Ia 22.7% and aac (3)‐Ib 17%. In addition, sixteen different patterns of AME genes were observed.ConclusionMost investigated isolates of K. pneumoniae were positive for different virulence‐associated and AME genes and therefore can play a significant role in life‐threatening infections. Meanwhile, resistance rates to aminoglycoside antibiotics were high and it was primarily due to the presence of AME genes such as aph (3″)‐Ib, ant (2″)‐Ia, and aac (3)‐Ib.
Background: The prevalence of multidrug-resistant Klebsiella pneumoniae (MDR-KP) is rising globally. The aim of this study was to investigate the epidemiology, risk factors and clinical outcomes of MDR-KP coinfections and infections with carbapenem-resistant Klebsiella pneumoniae (CRKP) among patients in a tertiary hospital in China, and to establish an individualized linear prediction model. Methods:In this retrospective study,patients admitted between January 2021 and March 2024 with a diagnosis of MDR-KP infection were included. Werecorded demographics, comorbidities, laboratory indicators, therapeutic interventions, antibiotic susceptibility results (AST) and analyzed clinical outcomes.Logistic regression models were employed to evaluate the risk factors associated with MDR-KP coinfections andinfections with CRKP. Results: A total of 164 patients with MDR-KP infection were included. Of these patients, 78 (47.6%) were infected with MDR-KP only and 86 (52.4%) were coinfected with other microbes; 115 (70.1%) were infected with extended-spectrum beta-lactamase producing Klebsiella pneumoniae (ESBL-KP), and 49 (29.9%) were infected with CRKP. The most common source of infection in patients with MDR-KP infection was the respiratory tract (96/164, 58.5%), followed by the urinary tract (31/164, 18.9%). Multivariate logistic regression analysis showed that nasogastric catheters (OR 5.351, 95% CI 1.437-19.926, P= 0.012),as well as venous and arterial catheters (OR 5.182, 95% CI 1.272-21.113, P = 0.022) were independent risk factors for coinfection. The total risk score for all factors was 143.3, with a predicted risk rate ranging from 0.25 to 0.85. In the ROC curve analysis, the area under the curve (AUC) for predicting coinfection using the total risk score was 0.773 (95% CI: 0.7054-0.8405). Tracheostomy (OR 4.673, 95% CI 1.153-18.937, P = 0.031) and fiberoptic bronchoscopy (OR 4.041, 95% CI 1.305-12.516, P = 0.015) were independent risk factors for infecting with CRKP, witha total risk score for all factors of 193.9, and a predicted risk rate ranging from 0.15 ~ 0.85. In the ROC curve analysis, the area under the curve (AUC) for predicting CRKP using the total risk score was 0.752 (95% CI: 0.6739-0.8306). Analysis on the calibration curve indicated good agreement between the observed and predicted values. The log-rank test was used to compare all-cause mortality between the two groups, and 30-day mortality was higher in the coinfected group than in the MDR-KP alone group (P = 0.03). There was no significant difference in 30-day mortality between the CRKP group and ESBL-KP group (P = 0.09). Conclusion: This study successfully established a model based on risk factors, which has good predictive value for both patients with coinfections and those with CRKP. Coinfections and CRKP infections significantly increased overall mortality and economic burden, while leading to poor prognosis in patients. These findings provided a basis for further clinical research and refinement of strategies for managing MDR-KP coinfections and CRKP infections.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.